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  • Molecular assay reagents intended to identify mutations in the serine/threonine kinase 11 (STK11) gene, located at chromosome 19p13.3, which encodes for a member of the serine/threonine kinase family, regulates cell polarity, and functions as a tumor suppressor. This inherited genetic mutation has been identified in patients with Peutz-Jeghers syndrome (PJS).
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